R&D Formulation Manager
Patras, Western Greece, GreeceRemote
AI Summary
Leads and oversees formulation development for generic pharmaceutical products, managing laboratory-scale development through scale-up and technology transfer.
About this role
VIANEX S.A., the leading Greek pharmaceutical company, is looking to hire an R&D Formulation Manager for its state-of-the-art R&D Center, based in Patras.
About the Role
The successful candidate will be responsible for leading and overseeing formulation development activities for generic pharmaceutical products across different dosage forms, from laboratory-scale development through scale-up and technology transfer.
Requirements
Key Responsibilities
- Lead and oversee formulation development activities for generic pharmaceutical products across different dosage forms.
- Design and develop robust formulations based on QTPP, CQAs, target product characteristics and regulatory requirements.
- Plan, coordinate and supervise formulation development trials from laboratory scale through scale-up and technology transfer.
- Lead formulation optimization activities and support the optimization of manufacturing process parameters.
- Coordinate the preparation, review and maintenance of formulation development protocols, reports and records.
- Ensure that formulation development activities are conducted in accordance with applicable GMP requirements, ICH guidelines, pharmacopoeial requirements and internal procedures.
- Contribute to the continuous improvement of formulation development approaches, processes and laboratory practices.
- Coordinate multiple formulation development projects, ensuring alignment with established timelines and development objectives.
- Collaborate effectively with cross-functional teams throughout the pharmaceutical development process.
Qualifications & Experience
- BSc or MSc Degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering or a related scientific discipline.
- 5–7 years of relevant professional experience in pharmaceutical formulation development, with proven experience in a similar position.
- Proven experience in the development of generic pharmaceutical products and formulation optimization.
- Experience with different pharmaceutical dosage forms, including immediate-release, modified-release, oral solutions and ODTs.
- Proven experience in scale-up, process optimization and technology transfer from laboratory to manufacturing scale.
- Demonstrated ability to lead multidisciplinary teams and coordinate multiple development projects within defined timelines.
- Excellent communication and collaboration skills, with the ability to work effectively with cross-functional teams.
- Good written and verbal communication skills in English.
Benefits
- Excellent working environment
- Competitive remuneration package
- Opportunities for professional development
Skills
CQAsDosage FormsGMPICH GuidelinesImmediate-releaseModified-releaseODTSOral SolutionsPharmaceutical Formulation DevelopmentPharmacopoeial RequirementsProcess OptimizationProject CoordinationQTPPScale-upTechnology Transfer
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